The immunization protocol determines whether endogenous interferon-γ suppresses the infiltration of eosinophils into the conjunctiva

Studies with interferon-γ knockout (GKO) mice showed that endogenous IFN-γ suppresses the infiltration of inflammatory cells into the conjunctiva. To examine whether this phenomenon is universally true, we induced conjunctival inflammation by four different immunization protocols. Both wild type (WT...

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Published inImmunology Letters Vol. 100; no. 2; pp. 189 - 194
Main Authors Fukushima, Atsuki, Yamaguchi, Tomoko, Ishida, Waka, Fukata, Kazuyo, Ozaki, Akemi, Ueno, Hisayuki
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 15.09.2005
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Abstract Studies with interferon-γ knockout (GKO) mice showed that endogenous IFN-γ suppresses the infiltration of inflammatory cells into the conjunctiva. To examine whether this phenomenon is universally true, we induced conjunctival inflammation by four different immunization protocols. Both wild type (WT) and GKO mice (C57BL/6 background) were immunized with ragweed (RW) in aluminum hydroxide (alum). Two different immunization protocols were used: either the emulsion was injected into only the left hind footpad or it was also injected into the tail base (50 μg RW in 2 mg alum per injection site). In addition, to compare the effects of the immunization dose of RW and the immunization site, 100 μg RW in 2 mg alum was injected into only the left hind footpad and 25 μg RW in 2 mg alum per injection site was injected into both the left hind footpad and the tail base. Ten days later, the mice were challenged with 2 mg RW in 10 μl PBS. Twenty-four hours later, the conjunctivas were analyzed histologically, and the cellular and humoral immune responses in the spleens and sera were determined, respectively. Similar to a previous report, GKO mice showed significant eosinophilic infiltration into the conjunctiva after the footpad only injection of 50 μg RW. However, injection of 50 μg RW per injection site into the footpad plus the tail base resulted in comparable levels of eosinophilic infiltration in WT and GKO mice. On the contrary, either immunization of 100 μg RW in 2 mg alum into only the left hind footpad or that of 25 μg RW in 2 mg alum into both the left hind footpad and the tail base induced significant infiltration of eosinophils into the conjunctiva of GKO mice, compared to WT mice. These results show that the immunization protocol employed has a marked effect on the severity of eosinophilic infiltration. These observations indicate that in interpreting experimental results in the study of EC, the immunization protocol employed must be considered.
AbstractList BACKGROUNDStudies with interferon-gamma knockout (GKO) mice showed that endogenous IFN-gamma suppresses the infiltration of inflammatory cells into the conjunctiva. To examine whether this phenomenon is universally true, we induced conjunctival inflammation by four different immunization protocols.METHODSBoth wild type (WT) and GKO mice (C57BL/6 background) were immunized with ragweed (RW) in aluminum hydroxide (alum). Two different immunization protocols were used: either the emulsion was injected into only the left hind footpad or it was also injected into the tail base (50 microg RW in 2mg alum per injection site). In addition, to compare the effects of the immunization dose of RW and the immunization site, 100 microg RW in 2mg alum was injected into only the left hind footpad and 25 microg RW in 2mg alum per injection site was injected into both the left hind footpad and the tail base. Ten days later, the mice were challenged with 2mg RW in 10 microl PBS. Twenty-four hours later, the conjunctivas were analyzed histologically, and the cellular and humoral immune responses in the spleens and sera were determined, respectively.RESULTSSimilar to a previous report, GKO mice showed significant eosinophilic infiltration into the conjunctiva after the footpad only injection of 50 microg RW. However, injection of 50 microg RW per injection site into the footpad plus the tail base resulted in comparable levels of eosinophilic infiltration in WT and GKO mice. On the contrary, either immunization of 100 microg RW in 2mg alum into only the left hind footpad or that of 25 microg RW in 2mg alum into both the left hind footpad and the tail base induced significant infiltration of eosinophils into the conjunctiva of GKO mice, compared to WT mice.CONCLUSIONSThese results show that the immunization protocol employed has a marked effect on the severity of eosinophilic infiltration. These observations indicate that in interpreting experimental results in the study of EC, the immunization protocol employed must be considered.
Background:: Studies with interferon- gamma knockout (GKO) mice showed that endogenous IFN- gamma suppresses the infiltration of inflammatory cells into the conjunctiva. To examine whether this phenomenon is universally true, we induced conjunctival inflammation by four different immunization protocols. Methods:: Both wild type (WT) and GKO mice (C57BL/6 background) were immunized with ragweed (RW) in aluminum hydroxide (alum). Two different immunization protocols were used: either the emulsion was injected into only the left hind footpad or it was also injected into the tail base (50 mu g RW in 2mg alum per injection site). In addition, to compare the effects of the immunization dose of RW and the immunization site, 100 mu g RW in 2mg alum was injected into only the left hind footpad and 25 mu g RW in 2mg alum per injection site was injected into both the left hind footpad and the tail base. Ten days later, the mice were challenged with 2mg RW in 10 mu l PBS. Twenty-four hours later, the conjunctivas were analyzed histologically, and the cellular and humoral immune responses in the spleens and sera were determined, respectively. Results:: Similar to a previous report, GKO mice showed significant eosinophilic infiltration into the conjunctiva after the footpad only injection of 50 mu g RW. However, injection of 50 mu g RW per injection site into the footpad plus the tail base resulted in comparable levels of eosinophilic infiltration in WT and GKO mice. On the contrary, either immunization of 100 mu g RW in 2mg alum into only the left hind footpad or that of 25 mu g RW in 2mg alum into both the left hind footpad and the tail base induced significant infiltration of eosinophils into the conjunctiva of GKO mice, compared to WT mice. Conclusions:: These results show that the immunization protocol employed has a marked effect on the severity of eosinophilic infiltration. These observations indicate that in interpreting experimental results in the study of EC, the immunization protocol employed must be considered.
Studies with interferon-γ knockout (GKO) mice showed that endogenous IFN-γ suppresses the infiltration of inflammatory cells into the conjunctiva. To examine whether this phenomenon is universally true, we induced conjunctival inflammation by four different immunization protocols. Both wild type (WT) and GKO mice (C57BL/6 background) were immunized with ragweed (RW) in aluminum hydroxide (alum). Two different immunization protocols were used: either the emulsion was injected into only the left hind footpad or it was also injected into the tail base (50 μg RW in 2 mg alum per injection site). In addition, to compare the effects of the immunization dose of RW and the immunization site, 100 μg RW in 2 mg alum was injected into only the left hind footpad and 25 μg RW in 2 mg alum per injection site was injected into both the left hind footpad and the tail base. Ten days later, the mice were challenged with 2 mg RW in 10 μl PBS. Twenty-four hours later, the conjunctivas were analyzed histologically, and the cellular and humoral immune responses in the spleens and sera were determined, respectively. Similar to a previous report, GKO mice showed significant eosinophilic infiltration into the conjunctiva after the footpad only injection of 50 μg RW. However, injection of 50 μg RW per injection site into the footpad plus the tail base resulted in comparable levels of eosinophilic infiltration in WT and GKO mice. On the contrary, either immunization of 100 μg RW in 2 mg alum into only the left hind footpad or that of 25 μg RW in 2 mg alum into both the left hind footpad and the tail base induced significant infiltration of eosinophils into the conjunctiva of GKO mice, compared to WT mice. These results show that the immunization protocol employed has a marked effect on the severity of eosinophilic infiltration. These observations indicate that in interpreting experimental results in the study of EC, the immunization protocol employed must be considered.
Studies with interferon-gamma knockout (GKO) mice showed that endogenous IFN-gamma suppresses the infiltration of inflammatory cells into the conjunctiva. To examine whether this phenomenon is universally true, we induced conjunctival inflammation by four different immunization protocols. Both wild type (WT) and GKO mice (C57BL/6 background) were immunized with ragweed (RW) in aluminum hydroxide (alum). Two different immunization protocols were used: either the emulsion was injected into only the left hind footpad or it was also injected into the tail base (50 microg RW in 2mg alum per injection site). In addition, to compare the effects of the immunization dose of RW and the immunization site, 100 microg RW in 2mg alum was injected into only the left hind footpad and 25 microg RW in 2mg alum per injection site was injected into both the left hind footpad and the tail base. Ten days later, the mice were challenged with 2mg RW in 10 microl PBS. Twenty-four hours later, the conjunctivas were analyzed histologically, and the cellular and humoral immune responses in the spleens and sera were determined, respectively. Similar to a previous report, GKO mice showed significant eosinophilic infiltration into the conjunctiva after the footpad only injection of 50 microg RW. However, injection of 50 microg RW per injection site into the footpad plus the tail base resulted in comparable levels of eosinophilic infiltration in WT and GKO mice. On the contrary, either immunization of 100 microg RW in 2mg alum into only the left hind footpad or that of 25 microg RW in 2mg alum into both the left hind footpad and the tail base induced significant infiltration of eosinophils into the conjunctiva of GKO mice, compared to WT mice. These results show that the immunization protocol employed has a marked effect on the severity of eosinophilic infiltration. These observations indicate that in interpreting experimental results in the study of EC, the immunization protocol employed must be considered.
Author Fukushima, Atsuki
Ishida, Waka
Ozaki, Akemi
Yamaguchi, Tomoko
Fukata, Kazuyo
Ueno, Hisayuki
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crossref_primary_10_1016_j_exer_2005_06_010
crossref_primary_10_1016_j_imlet_2006_07_001
Cites_doi 10.1126/science.8456300
10.1006/clin.1997.4507
10.1046/j.1398-9995.2003.00326.x
10.1016/S0091-6749(00)90080-0
10.1136/bjo.86.10.1166
10.1002/ana.410360714
10.1016/0090-1229(87)90133-4
10.1080/02713680590927560
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Keywords Interferon-gamma
Allergic conjunctivitis
Knockout mouse
Active immunization
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References Magone, Whitcup, Fukushima, Chan, Silver, Rizzo (bib5) 2000; 105
Fukushima, Ozaki, Jian, Ishida, Fukata, Liu, Ueno (bib8) 2005; 30
Magone, Chan, Rizzo, Kozhich, Whitcup (bib4) 1998; 87
Groneberg, Bielory, Fischer, Bonini, Wahn (bib3) 2003; 58
Dalton, Pitts-Meek, Keshav, Figari, Bradley, Stewart (bib7) 1993; 259
Agarwal, Caspi (bib9) 2004; 102
Fukushima, Fukata, Ozaki, Takata, Kuroda, Enzan, Ueno (bib6) 2002; 86
Wekerle, Kojima, Lannes-Vieira, Lassmann, Linington (bib1) 1994; 36
Fox, Kuwabara, Wiggert, Redmond, Hess, Chader, Gery (bib2) 1987; 43
Magone (10.1016/j.imlet.2005.04.012_bib5) 2000; 105
Fox (10.1016/j.imlet.2005.04.012_bib2) 1987; 43
Fukushima (10.1016/j.imlet.2005.04.012_bib6) 2002; 86
Wekerle (10.1016/j.imlet.2005.04.012_bib1) 1994; 36
Magone (10.1016/j.imlet.2005.04.012_bib4) 1998; 87
Fukushima (10.1016/j.imlet.2005.04.012_bib8) 2005; 30
Agarwal (10.1016/j.imlet.2005.04.012_bib9) 2004; 102
Groneberg (10.1016/j.imlet.2005.04.012_bib3) 2003; 58
Dalton (10.1016/j.imlet.2005.04.012_bib7) 1993; 259
References_xml – volume: 86
  start-page: 1166
  year: 2002
  end-page: 1171
  ident: bib6
  article-title: Exertion of the suppressive effects of IFN-gamma on experimental immune mediated blepharoconjunctivitis in Brown Norway rats during the induction phase but not the effector phase
  publication-title: Br J Ophthalmol
  contributor:
    fullname: Ueno
– volume: 58
  start-page: 1101
  year: 2003
  end-page: 1113
  ident: bib3
  article-title: Animal models of allergic and inflammatory conjunctivitis
  publication-title: Allergy
  contributor:
    fullname: Wahn
– volume: 102
  start-page: 395
  year: 2004
  end-page: 420
  ident: bib9
  article-title: Rodent models of experimental autoimmune uveitis
  publication-title: Meth Mol Med
  contributor:
    fullname: Caspi
– volume: 43
  start-page: 256
  year: 1987
  end-page: 264
  ident: bib2
  article-title: Experimental autoimmune uveoretinitis (EAU) induced by retinal interphotoreceptor retinoid-binding protein (IRBP): differences between EAU induced by IRBP and by S-antigen
  publication-title: Clin Immunol Immunopathol
  contributor:
    fullname: Gery
– volume: 30
  start-page: 241
  year: 2005
  end-page: 248
  ident: bib8
  article-title: Dissection of antigen-specific humoral and cellular immune responses for the development of experimental immune-mediated blepharoconjunctivitis (EC) in C57BL/6 mice
  publication-title: Curr Eye Res
  contributor:
    fullname: Ueno
– volume: 259
  start-page: 1739
  year: 1993
  end-page: 1742
  ident: bib7
  article-title: Multiple defects of immune cell function in mice with disrupted interferon-gamma genes
  publication-title: Science
  contributor:
    fullname: Stewart
– volume: 36
  start-page: 47
  year: 1994
  end-page: 53
  ident: bib1
  article-title: Animal models
  publication-title: Ann Neurol
  contributor:
    fullname: Linington
– volume: 105
  start-page: 299
  year: 2000
  end-page: 308
  ident: bib5
  article-title: The role of IL-12 in the induction of late-phase cellular infiltration in a murine model of allergic conjunctivitis
  publication-title: J Allergy Clin Immunol
  contributor:
    fullname: Rizzo
– volume: 87
  start-page: 75
  year: 1998
  end-page: 84
  ident: bib4
  article-title: A novel murine model of allergic conjunctivitis
  publication-title: Clin Immunol Immunopathol
  contributor:
    fullname: Whitcup
– volume: 259
  start-page: 1739
  year: 1993
  ident: 10.1016/j.imlet.2005.04.012_bib7
  article-title: Multiple defects of immune cell function in mice with disrupted interferon-gamma genes
  publication-title: Science
  doi: 10.1126/science.8456300
  contributor:
    fullname: Dalton
– volume: 87
  start-page: 75
  year: 1998
  ident: 10.1016/j.imlet.2005.04.012_bib4
  article-title: A novel murine model of allergic conjunctivitis
  publication-title: Clin Immunol Immunopathol
  doi: 10.1006/clin.1997.4507
  contributor:
    fullname: Magone
– volume: 58
  start-page: 1101
  year: 2003
  ident: 10.1016/j.imlet.2005.04.012_bib3
  article-title: Animal models of allergic and inflammatory conjunctivitis
  publication-title: Allergy
  doi: 10.1046/j.1398-9995.2003.00326.x
  contributor:
    fullname: Groneberg
– volume: 105
  start-page: 299
  year: 2000
  ident: 10.1016/j.imlet.2005.04.012_bib5
  article-title: The role of IL-12 in the induction of late-phase cellular infiltration in a murine model of allergic conjunctivitis
  publication-title: J Allergy Clin Immunol
  doi: 10.1016/S0091-6749(00)90080-0
  contributor:
    fullname: Magone
– volume: 86
  start-page: 1166
  year: 2002
  ident: 10.1016/j.imlet.2005.04.012_bib6
  article-title: Exertion of the suppressive effects of IFN-gamma on experimental immune mediated blepharoconjunctivitis in Brown Norway rats during the induction phase but not the effector phase
  publication-title: Br J Ophthalmol
  doi: 10.1136/bjo.86.10.1166
  contributor:
    fullname: Fukushima
– volume: 36
  start-page: 47
  issue: Suppl.
  year: 1994
  ident: 10.1016/j.imlet.2005.04.012_bib1
  article-title: Animal models
  publication-title: Ann Neurol
  doi: 10.1002/ana.410360714
  contributor:
    fullname: Wekerle
– volume: 43
  start-page: 256
  year: 1987
  ident: 10.1016/j.imlet.2005.04.012_bib2
  article-title: Experimental autoimmune uveoretinitis (EAU) induced by retinal interphotoreceptor retinoid-binding protein (IRBP): differences between EAU induced by IRBP and by S-antigen
  publication-title: Clin Immunol Immunopathol
  doi: 10.1016/0090-1229(87)90133-4
  contributor:
    fullname: Fox
– volume: 30
  start-page: 241
  year: 2005
  ident: 10.1016/j.imlet.2005.04.012_bib8
  article-title: Dissection of antigen-specific humoral and cellular immune responses for the development of experimental immune-mediated blepharoconjunctivitis (EC) in C57BL/6 mice
  publication-title: Curr Eye Res
  doi: 10.1080/02713680590927560
  contributor:
    fullname: Fukushima
– volume: 102
  start-page: 395
  year: 2004
  ident: 10.1016/j.imlet.2005.04.012_bib9
  article-title: Rodent models of experimental autoimmune uveitis
  publication-title: Meth Mol Med
  contributor:
    fullname: Agarwal
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Snippet Studies with interferon-γ knockout (GKO) mice showed that endogenous IFN-γ suppresses the infiltration of inflammatory cells into the conjunctiva. To examine...
Studies with interferon-gamma knockout (GKO) mice showed that endogenous IFN-gamma suppresses the infiltration of inflammatory cells into the conjunctiva. To...
Background:: Studies with interferon- gamma knockout (GKO) mice showed that endogenous IFN- gamma suppresses the infiltration of inflammatory cells into the...
BACKGROUNDStudies with interferon-gamma knockout (GKO) mice showed that endogenous IFN-gamma suppresses the infiltration of inflammatory cells into the...
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SubjectTerms Active immunization
Allergens - immunology
Allergic conjunctivitis
Ambrosia
Animals
Cell Proliferation
Cells, Cultured
Conjunctivitis, Allergic - etiology
Conjunctivitis, Allergic - immunology
Conjunctivitis, Allergic - pathology
Dose-Response Relationship, Immunologic
Eosinophils - immunology
Immunization - methods
Immunoglobulin E - blood
Interferon-gamma
Interferon-gamma - genetics
Interferon-gamma - immunology
Interleukin-4 - biosynthesis
Knockout mouse
Mice
Mice, Inbred C57BL
Mice, Knockout
Pollen - immunology
Spleen - cytology
Spleen - immunology
Spleen - metabolism
Title The immunization protocol determines whether endogenous interferon-γ suppresses the infiltration of eosinophils into the conjunctiva
URI https://dx.doi.org/10.1016/j.imlet.2005.04.012
https://www.ncbi.nlm.nih.gov/pubmed/15919119
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